Spar
PAT Applied in Biopharmaceutical Process Development And Manufacturing
e-bok, 2011
Engelsk
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As with all of pharmaceutical production, the regulatory environment for the production of therapeutics has been changing as a direct result of the US FDA-initiated Quality by Design (QbD) guidelines and corresponding activities of the International Committee for Harmonization (ICH). Given the rapid growth in the biopharmaceutical area and the comp
- Undertittel
- An Enabling Tool for Quality-by-Design
- Redaktør
- Duncan Low, Jose C. Menezes, Mel Koch, Cenk Undey
- ISBN
- 9781439829462
- Språk
- Engelsk
- Utgivelsesdato
- 7.12.2011
- Forlag
- CRC PRESS
- Tilgjengelige elektroniske format
- PDF - Adobe DRM
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- Lesebrett
- Datamaskin
